Canonical Allele Identifier: CA1272522478

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254835_96254836delinsGT , CM000664.2:g.96254835_96254836delinsGT	GRCh38
NC_000002.11:g.96920573_96920574delinsGT , CM000664.1:g.96920573_96920574delinsGT	GRCh37
NC_000002.10:g.96284300_96284301delinsGT	NCBI36
NG_027695.1:g.16178_16179delinsAC , LRG_528:g.16178_16179delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.406_407delinsAC MANE Select	ENSP00000258439.3:p.Thr136=
ENST00000258439.7:c.406_407delinsAC	ENSP00000258439.2:p.Thr136=
ENST00000432959.1:c.406_407delinsAC	ENSP00000416660.1:p.Thr136=
ENST00000435268.1:c.154_155delinsAC	ENSP00000411810.1:p.Thr52=
NM_001193304.2:c.406_407delinsAC	NP_001180233.1:p.Thr136=
NM_017849.3:c.406_407delinsAC , LRG_528t1:c.406_407delinsAC	NP_060319.1:p.Thr136=
XM_017004450.1:c.-513_-512delinsAC	XP_016859939.1:n.-513_-512delinsAC
XM_017004452.1:c.154_155delinsAC	XP_016859941.1:p.Thr52=
NM_001193304.3:c.406_407delinsAC	NP_001180233.1:p.Thr136=
NM_017849.4:c.406_407delinsAC MANE Select	NP_060319.1:p.Thr136=